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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3118102copy number variation23nstd145human GRCh37 chr14: 41,610,669-41,668,279 , GRCh38.p12 chr14: 41,141,466-41,199,076 LINC02315
    nsv3117809copy number variation152nstd145human GRCh37 chr20: 1,561,593-1,584,273 , GRCh38.p12 chr20: 1,580,947-1,603,627 SIRPB1
    nsv3117354copy number variation83nstd145human GRCh37 chr17: 15,043,995-15,058,468 , GRCh38.p12 chr17: 15,140,678-15,155,151 LOC107984976
    nsv3114057copy number variation160nstd145human GRCh37 chr19: 52,134,789-52,148,550 , GRCh38.p12 chr19: 51,631,536-51,645,297 SIGLEC14
    nsv3115697copy number variation53nstd145human GRCh37 chr11: 7,814,824-7,826,930 , GRCh38.p12 chr11: 7,793,277-7,805,383 , GRCh38.p12 chr11|NT_187583.1: 14,145-26,251 , GRCh38.p12 chr11|NW_011332695.1: 14,145-26,251 OR5P2
    nsv3112094copy number variation94nstd145human GRCh37 chr7: 133,785,285-133,797,218 , GRCh38.p12 chr7: 134,100,532-134,112,465
    nsv3110986copy number variation37nstd145human GRCh37 chr5: 17,640,200-17,651,341 , GRCh38.p12 chr5: 17,640,091-17,651,232 LOC391768
    nsv3115789copy number variation1nstd145human GRCh37 chr19: 2,801,546-2,812,079 , GRCh38.p12 chr19: 2,801,548-2,812,081 THOP1
    nsv3114521copy number variation39nstd145human GRCh37 chr18: 66,745,828-66,756,183 , GRCh38.p12 chr18: 69,078,591-69,088,946 CCDC102B
    nsv3113383copy number variation199nstd145human GRCh37 chr3: 192,875,554-192,885,008 , GRCh38.p12 chr3: 193,157,765-193,167,219 VEZF1P1
    nsv3114654copy number variation2nstd145human GRCh37 chr3: 37,977,700-37,986,922 , GRCh38.p12 chr3: 37,936,209-37,945,431 CTDSPL
    nsv3115609copy number variation20nstd145human GRCh37 chr1: 222,373,920-222,382,729 , GRCh38.p12 chr1: 222,200,578-222,209,387 CFAP144P3
    nsv3116985copy number variation1nstd145human GRCh37 chr22: 28,190,952-28,199,103 , GRCh38.p12 chr22: 27,794,964-27,803,115 MN1
    nsv3116004copy number variation19nstd145human GRCh37 chr1: 152,762,880-152,769,856 , GRCh38.p12 chr1: 152,790,404-152,797,380 LCE1D
    nsv3112878copy number variation1nstd145human GRCh37 chr19: 42,753,998-42,760,925 , GRCh38.p12 chr19: 42,249,846-42,256,773 ERF
    nsv3116211copy number variation4nstd145human GRCh37 chr8: 3,996,734-4,003,457 , GRCh38.p12 chr8: 4,139,212-4,145,935 CSMD1
    nsv3116108copy number variation1nstd145human GRCh37 chr15: 82,334,966-82,341,405 , GRCh38.p12 chr15: 82,042,625-82,049,064 MEX3B
    nsv3112895copy number variation76nstd145human GRCh37 chr12: 43,020,941-43,027,293 , GRCh38.p12 chr12: 42,627,139-42,633,491 LINC02402
    nsv3118170copy number variation1nstd145human GRCh37 chr19: 42,771,801-42,777,696 , GRCh38.p12 chr19: 42,267,649-42,273,544 CIC
    nsv3113533copy number variation5nstd145human GRCh37 chr20: 58,670,144-58,675,640 , GRCh38.p12 chr20: 60,095,089-60,100,585 LOC729296
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